RegWardenFDA facility compliance records
Facility

BSN-JOBST GMBH

1 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2018: 1 inspections; 2022: 1 recalls; 2023: 1 inspections2017120182019202020211202212023202420252026
  • Recalls (1)
  • Inspections (2)

Devices registered here (1)

  • Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)
    Product code DWL (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5780

Recalls & enforcement

  • Class IITerminated2022-02-01
    The folding boxes within the shipping case are mislabeled. The shipping case and immediate packages within the folding boxes are correctly labeled.

FDA inspections (2)

  • NAI2023-02-22
    No Action Indicated · Compliance: Devices
  • NAI2018-03-07
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “BSN-JOBST GMBH (FEI 3005588760) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3005588760-bsn-jobst-gmbh/

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